Canonical Allele Identifier: CA389643925

Gene: SOS2

Linked Data

• MyVariant Identifiers: chr14:g.50616886G>A (hg19) ; chr14:g.50150168G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.50150168G>A , CM000676.2:g.50150168G>A	GRCh38
NC_000014.8:g.50616886G>A , CM000676.1:g.50616886G>A	GRCh37
NC_000014.7:g.49686636G>A	NCBI36
NG_051073.1:g.86526C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000216373.10:c.2224C>T MANE Select	ENSP00000216373.5:p.Gln742Ter
ENST00000216373.9:c.2224C>T	ENSP00000216373.5:p.Gln742Ter
ENST00000543680.5:c.2125C>T	ENSP00000445328.1:p.Gln709Ter
NM_006939.2:c.2224C>T	NP_008870.2:p.Gln742Ter
XM_005268021.1:c.2044C>T	XP_005268078.1:p.Gln682Ter
XM_011537103.1:c.2185C>T	XP_011535405.1:p.Gln729Ter
XM_011537104.1:c.2224C>T	XP_011535406.1:p.Gln742Ter
NM_006939.3:c.2224C>T	NP_008870.2:p.Gln742Ter
NM_006939.4:c.2224C>T MANE Select	NP_008870.2:p.Gln742Ter